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Data / Medical devices / Lens, Spectacle (Prescription), For Reading Discomfort / United States

FDA-registered makers of Lens, Spectacle (Prescription), For Reading Discomfort in the United States: 21 establishments

21 establishments in the United States are registered with the FDA to make Lens, Spectacle (Prescription), For Reading Discomfort (product code NJH). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Lens, Spectacle (Prescription), For Reading Discomfort
Product code
NJH
Country
United States

Makers of Lens, Spectacle (Prescription), For Reading Discomfort in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Alpha Manufacturing Group IncMaspeth, NY, United StatesContract manufacturer0000api.fda.gov
Benny's EyewearBloomfield Hills, MI, United StatesSpecification developer0000api.fda.gov
CC Ops, LLCProspect, KY, United StatesSpecification developer0000api.fda.gov
Eason Eyewear Inc.Hempstead, NY, United StatesRemanufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Essilor Laboratories of America, Inc. dba Omega Northcreek LabDallas, TX, United StatesManufacturer0000api.fda.gov
Glassesusa Fulfillment Center, Inc.College Park, GA, United StatesComplaint file establishment, Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Global Source RXScottsdale, AZ, United StatesRepackager or relabeler, Reprocessor0000api.fda.gov
Gunnar OptiksOceanside, CA, United StatesSpecification developer0000api.fda.gov
Nicefy IncTorrance, CA, United StatesSpecification developer0000api.fda.gov
Ogi, LLCNew Hope, MN, United StatesSpecification developer0000api.fda.gov
Olivio IncIrvine, CA, United StatesManufacturer0000api.fda.gov
PDS OpticalLouisville, KY, United StatesManufacturer0000api.fda.gov
PDS Optical FloridaFort Lauderdale, FL, United StatesManufacturer0000api.fda.gov
Phillips Safety Products, Inc.Middlesex, NJ, United StatesManufacturer0000api.fda.gov
Smith Sport Optics, Inc.Clearfield, UT, United StatesContract manufacturer, Manufacturer, Remanufacturer, Repackager or relabeler0000api.fda.gov
Summer Hawk OpticsBuda, TX, United StatesManufacturer, Remanufacturer, Repackager or relabeler0000api.fda.gov
Three Rivers OpticalPittsburgh, PA, United StatesManufacturer, Repackager or relabeler, Reprocessor0000api.fda.gov
Vision RX Lab America LLCCranford, NJ, United StatesRemanufacturer0000api.fda.gov
Wal-Mart Optical LabFayetteville, AR, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Walmart Optical LabDallas, TX, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Zenni Usa, Inc.Obetz, OH, United StatesManufacturer, Repackager or relabeler0000api.fda.gov

Updated November 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.